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65389002: Adrenoleukodystrophy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
108634018 Adrenoleukodystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
108635017 Adrenomyeloneuropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
108637013 Bronze Schilder disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
108638015 Schilder-Addison complex en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
108639011 Siemerling-Creutzfeldt disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1232670018 X-linked adrenoleucodystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2154288010 Adrenoleucodystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2957107010 ALD - adrenoleukodystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4637154010 X-linked adrenoleukodystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
804886014 Adrenoleukodystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Adrenoleukodystrophy est un(e) (attribut) X-linked dominant hereditary disease (disorder) true Inferred relationship Some
Adrenoleukodystrophy est un(e) (attribut) Adrenal cortical hypofunction (disorder) true Inferred relationship Some
Adrenoleukodystrophy est un(e) (attribut) Loss of single peroxisomal function true Inferred relationship Some
Adrenoleukodystrophy est un(e) (attribut) Adrenal cortical hypofunction false Inferred relationship Some
Adrenoleukodystrophy est un(e) (attribut) Congenital anomaly of adrenal gland false Inferred relationship Some
Adrenoleukodystrophy est un(e) (attribut) Hereditary disorder of endocrine system (disorder) true Inferred relationship Some
Adrenoleukodystrophy est un(e) (attribut) Reproductive system hereditary disorder false Inferred relationship Some
Adrenoleukodystrophy survenue (attribut) congénital true Inferred relationship Some 1
Adrenoleukodystrophy localisation d'une constatation (attribut) cortex surrénalien true Inferred relationship Some 1
Adrenoleukodystrophy localisation d'une constatation (attribut) Entire endocrine gonad (body structure) false Inferred relationship Some
Adrenoleukodystrophy localisation d'une constatation (attribut) cortex surrénalien false Inferred relationship Some
Adrenoleukodystrophy survenue (attribut) congénital false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Neonatal adrenoleukodystrophy est un(e) (attribut) True Adrenoleukodystrophy Inferred relationship Some
Acyl-coenzyme A oxidase deficiency (disorder) est un(e) (attribut) False Adrenoleukodystrophy Inferred relationship Some
Adolescent X-linked adrenoleukodystrophy (disorder) est un(e) (attribut) True Adrenoleukodystrophy Inferred relationship Some
Childhood cerebral X-linked adrenoleukodystrophy est un(e) (attribut) True Adrenoleukodystrophy Inferred relationship Some

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

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